US11617793B2ActiveUtilityA1
Anhydrous sodium thiosulfate and formulations thereof
Est. expiryJul 3, 2038(~12 yrs left)· nominal 20-yr term from priority
Inventors:Thomas Claiborne LovelaceJoseph A. Moore, IiiChristopher Mckinnon LeeDaniel Logan Kirschner
A61K 47/26A61K 47/02A61K 47/183A61K 47/18A61K 33/04A61K 9/19C01B 17/64A61K 9/0019A61K 33/243A61P 35/00A61K 47/20A61K 9/08C01P 2002/72
94
PatentIndex Score
3
Cited by
111
References
8
Claims
Abstract
Described herein is anhydrous sodium thiosulfate, methods for synthesizing anhydrous sodium thiosulfate, pharmaceutical compositions thereof, and methods of treating ototoxicity. Anhydrous sodium thiosulfate is synthesized from sodium sulfite, sulfur, and cetylpyridinium chloride. The anhydrous sodium thiosulfate is formulated into a pharmaceutical composition comprising a buffer and solvent. These compositions are useful for eliminating or reducing ototoxicity in pediatric patients receiving platinum-based chemotherapeutics.
Claims
exact text as granted — not AI-modifiedWhat is claimed:
1. A pharmaceutical composition comprising sodium thiosulfate at a concentration of about 0.5 M and further comprising about 0.004 M boric acid wherein the pharmaceutical composition has a pH between about 6.5 and about 8.9.
2. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition has a total volume of about 100 mL.
3. The pharmaceutical composition of claim 2 , wherein the pharmaceutical composition further comprises hydrochloric acid.
4. The pharmaceutical composition of claim 2 , wherein the pharmaceutical composition further comprises sodium hydroxide.
5. The pharmaceutical composition of claim 2 , wherein the pharmaceutical composition has a pH between about 8.6 and about 8.8.
6. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition further comprises hydrochloric acid.
7. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition further comprises sodium hydroxide.
8. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition has a pH between about 8.6 and about 8.8.Cited by (0)
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